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Exome-wide association study of plasma lipids in >300,000 individuals
Biological interpretation of genome-wide association studies using predicted gene functions
Autosomal dominant diabetes arising from a Wolfram syndrome 1 mutation
Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use
Fine mapping of five loci associated with low-density lipoprotein cholesterol detects variants that double the explained heritability
Analysis of protein-coding genetic variation in 60,706 humans
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk
Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls
Determinants of penetrance and variable expressivity in monogenic metabolic conditions across 77,184 exomes
Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps
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